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RAMP Procalcitonin - Taiwan Registration 76ff3dcbe23345fb5838bf29fd1ea888

Access comprehensive regulatory information for RAMP Procalcitonin in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 76ff3dcbe23345fb5838bf29fd1ea888 and manufactured by RESPONSE BIOMEDICAL CORPORATION. The authorized representative in Taiwan is RECHI CO., LTD..

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76ff3dcbe23345fb5838bf29fd1ea888
Registration Details
Taiwan FDA Registration: 76ff3dcbe23345fb5838bf29fd1ea888
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Device Details

RAMP Procalcitonin
TW: โ€œๅ€ซๆ™ฎโ€้™้ˆฃ็ด ๅŽŸๆชข้ฉ—่ฉฆๅŠ‘็ต„
Risk Class 2
MD

Registration Details

76ff3dcbe23345fb5838bf29fd1ea888

Ministry of Health Medical Device Import No. 031314

DHA05603131402

Company Information

Product Details

This product is used with RAMP instrument to quantitatively detect the content of procalcitonin in EDTA whole blood in vitro by immunochromocytometry.

C Immunology and microbiology devices

C3210 Endotoxin Analysis Reagent

Imported from abroad

Dates and Status

Jul 05, 2018

Jul 05, 2028